| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:36464151-36464492 | Common:2; Rare:110 | ||||
| chr1:37474363-37474521 | Common:1; Rare:56 | ||||
| chr1:37692214-37692564 | Common:4; Rare:78 | ||||
| chr1:38873301-38873563 | Common:3; Rare:93 | ||||
| chr1:39026238-39026390 | Common:1; Rare:38 | ||||
| chr1:39883441-39883575 | Common:1; Rare:55; Clinvar (pathogenic):1 | ||||
| chr1:40040437-40040831 | Common:3; Rare:119 | ||||
| chr1:40257909-40258264 | Common:4; Rare:95; Clinvar:7 | ||||
| chr1:40531487-40531721 | Common:1; Rare:64 | ||||
| chr1:40691504-40691812 | Common:2; Rare:149 | ||||
| chr1:42335165-42335349 | Common:3; Rare:96 | ||||
| chr1:42658273-42658511 | Common:2; Rare:74 | ||||
| chr1:42682611-42682731 | Common:1; Rare:46 | ||||
| chr1:42767029-42767303 | Common:3; Rare:78 | ||||
| chr1:42846392-42846638 | Common:1; Rare:68 |